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Updated: Jul 1, 2026

Implementation of In Vitro Drug Resistance Assays: Maximizing the Potential for Uncovering Clinically Relevant Resistance Mechanisms
Published on: December 9, 2015
Molecular studies on the impact of microbiome on anticancer drug resistance
Ke Zhou1,2,3, Ping Lu1,2,3, Hongli Xu1,2,3
1Department of Abdominal Oncology, Hubei Cancer Hospital, Tongji Medical College, Huazhong University of Science and Technology, Wuhan, China.
Abstract:
Cancer remains a leading global health challenge, with drug resistance posing a critical barrier to the durable efficacy of anticancer therapies, including chemotherapy, immunotherapy, and targeted treatments. Growing evidence highlights the gut microbiome as a key modulator in this resistance process. The gut microbiome-a dynamic and diverse microbial ecosystem-can influence drug efficacy through multiple mechanisms, including the biotransformation of chemotherapeutics, modulation of immune responses, alteration of host drug-metabolizing enzymes, and reshaping of the tumor microenvironment. Notably, specific bacterial taxa can enzymatically inactivate chemotherapeutic drugs, while microbial metabolites and signaling pathways further promote resistance by rewiring cellular survival and immune-regulatory programs. In this review, we synthesize recent molecular insights into microbiome-driven anticancer drug resistance and discuss emerging microbiome-targeted strategies, such as dietary intervention, probiotics and prebiotics, fecal microbiota transplantation, and advanced drug delivery systems. A deeper understanding of host-microbiome-drug interactions may provide new opportunities to overcome therapeutic resistance and advance precision oncology.
Insights
The gut microbiome significantly impacts cancer drug resistance by altering drug metabolism and immune responses. Targeting the microbiome offers new strategies to improve anticancer therapy effectiveness.
Area of Science:
- Oncology
- Microbiology
- Pharmacology
Background:
- Cancer drug resistance limits treatment efficacy.
- The gut microbiome influences various biological processes.
- Microbiome-cancer therapy interactions are increasingly recognized.
Purpose of the Study:
- To review molecular mechanisms of microbiome-driven anticancer drug resistance.
- To discuss emerging microbiome-targeted therapeutic strategies.
Main Methods:
- Literature review and synthesis of current research.
- Analysis of host-microbiome-drug interactions.
Main Results:
- The gut microbiome modulates anticancer drug efficacy through biotransformation, immune modulation, and TME alteration.
- Specific bacteria and microbial metabolites contribute to drug resistance.
- Microbiome dysbiosis can promote resistance by affecting host pathways.
Conclusions:
- Understanding host-microbiome-drug interactions is crucial for overcoming resistance.
- Microbiome-targeted strategies hold promise for enhancing precision oncology.
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